D68.52
BillableProthrombin gene mutation
D68.52 is the ICD-10-CM code for Prothrombin gene mutation. It is a billable, specific code valid for reimbursement.
D50-D89 Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism
What this means — in plain language
MedlinePlus · NIHNormally, if you get hurt, your body forms a blood clot to stop the bleeding . For blood to clot, your body needs cells called platelets and proteins known as clotting factors. If you have a bleeding disorder, you either do not have enough platelets or clotting factors or they don't work the way they should. Bleeding disorders can be the result of other diseases, such as severe liver disease or a lack of vitamin K .…
Read more about Bleeding Disorders at MedlinePlus ↗Source: U.S. National Library of Medicine (MedlinePlus). Informational only — not medical advice.
Medications indicated for this condition
FDA labeling- Desmopressin›
- vitamin K1Vitamin K [EPC]›
- ArgatrobanAnti-coagulant [EPC]›
- ADAMTS13, recombinant›
- Caplacizumab›
- factor X›
- Heparin Sodium in Sodium Chloride›
Drugs whose FDA labeling lists this condition's category among its indications. Informational only — not a treatment recommendation or medical advice.
Conditions mapped to this code
MedlinePlus · NIHPlain-language health-topic references grounded in MedlinePlus (NIH/NLM).
Frequently asked questions
- What is ICD-10 code D68.52?
- D68.52 is the ICD-10-CM code for "Prothrombin gene mutation". It falls under D50-D89 Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism.
- Is D68.52 a billable code?
- Yes — D68.52 is a billable, specific ICD-10-CM code valid for reimbursement.
Source: CMS ICD-10-CM FY2026. For informational purposes only — not medical advice. See our medical disclaimer.
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